Devices, Systems and Methods for Actuation and Retraction in Fluid Collection

ABSTRACT

The disclosed apparatus, systems and methods relate to devices, systems and methods for the collection of bodily fluids involving a single-use actuation and retraction mechanism disposed within a collector.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a continuation of U.S. patent application Ser. No.15/387,177, filed Dec. 21, 2016, and entitled “DEVICES, SYSTEMS ANDMETHODS FOR ACTUATION AND RETRACTION IN FLUID COLLECTION,” which claimsbenefit of U.S. Provisional Patent Application No. 62/270,550, filedDec. 21, 2015, and entitled “DEVICES, SYSTEMS AND METHODS FOR ACTUATIONAND RETRACTION IN FLUID COLLECTION,” the contents of which are herebyincorporated by reference in their entireties.

FEDERALLY SPONSORED RESEARCH OR DEVELOPMENT

This invention was made with government support under Contract#W31P4Q14C0006 awarded by DARPA. The government has certain rights inthe invention.

TECHNICAL FIELD

The disclosed technology relates generally to the collection of bodilyfluids, and in particular, to the devices, systems, and methodsproviding for the collection of bodily fluids into a receptacle and, incertain embodiments, utilizing force and energy minimums on the fluidbeing collected to add functionality by way of a guidance mechanism forfull lancet penetration, safe lancet storage and vacuum creation. Theseembodiments have implications for active fluid collection, safety andmanufacturing.

BACKGROUND

Devices, systems and methods to collect bodily fluids are necessarydevices for the growing field of personalized medicine. As point-of-caredevices continue to improve, an often overlooked area lies within thecollection of samples from untrained users. Currently, biologicalsamples are most commonly obtained via either simple-to-use methods ordevices, as with generic lancing devices, or trained personnel, as withphlebotomy venipunctures. In order to transfer the bodily fluid to acontainer, receptacle, or an analysis device, multiple steps arerequired that are time consuming, error prone and/or cumbersome.

Thus, there is a need in the art for improved microfluidic devices forfluid handling and transfer, and related systems and methods.

BRIEF SUMMARY

Discussed herein are various embodiments of the collection device, aswell as associated systems and methods for its use. For brevity, theseembodiments may be described in relation to a “collector,” though thatis not intended to limit the scope of the disclosure in any way.

In one Example a collector is provided including a housing includingproximal and distal ends and a lumen, an actuator disposed within thelumen, a platform disposed within the lumen and distal to the actuator,single use actuation mechanism in operational communication with theplatform, and a plunger including at least one lancet, wherein thesingle actuation mechanism is configured to translate linear forceapplied to the actuator into rotational force on the platform and urgethe plunger distally.

Implementations of this Example may include one or more of the followingfeatures. The collector further including a membrane disposed within thelumen, where the membrane is configured to create a fluidic seal withinthe lumen. The collector where the membrane includes a membrane lumenand a one way valve configured to create a vacuum within the membranelumen. The collector where the membrane includes a bellows. Thecollector where plunger is configured to retract after actuation. Thecollector where the platform includes at least one projection which isin operational communication with the single actuation mechanism. Thecollector where the single actuation mechanism includes at least oneactuator arm and at least one elongate guide. The collector where thesingle actuation mechanism is configured so as rotate the platformduring actuation by way of the projection. The collector where thehousing includes at least one elongate guide including a guide groove.The collector further including a spring configured urge the at leastone projection into the guide groove. The collector where the at leastone actuator arm is configured to urge the projection distally anddislodge it from the guide groove in response to actuation. Thecollector further including a variable width guide face. The collectorwhere the at least one projection includes a projection face configuredto rotate the platform when the projection is urged distally.

In another Example, a single use fluid collector is provided, including:a housing including proximal and distal ends and a lumen, an actuatorincluding at least one actuator arm disposed within the lumen, and aplatform including at least one projection disposed within the lumen anddistal to the actuator. The single use fluid collector also includeswhere the at least one actuator arm is in translational and rotationalcommunication with the platform via the at least one projection.

Implementations of this Example may include one or more of the followingfeatures. The collector where the housing includes at least one elongateguide including a guide groove. The collector further including a springconfigured urge the at least one projection into the guide groove. Thecollector where the at least one actuator arm is configured to urge theprojection distally and dislodge it from the guide groove in response toactuation. The collector further including a variable width guide face.The collector where the at least one projection includes a projectionface configured to rotate the platform when the projection is urgeddistally. The system where at least one actuator arm is in operationalcommunication with the at least one projection to translate linear forcefrom the arm into rotational force on the platform. The system where atleast one elongate guide includes a guide notch. The system where atleast one actuator arm includes an actuator catch. The system furtherincluding an actuation mechanism configured to increase platformresidence time. The system further including a membrane collar.

In another Example, an actuation and retraction system for use in amedical device is provided, the system including: a housing including acentral lumen extending through the housing and including at least oneelongate guide disposed within the central lumen, an actuator includingat least one actuator arm extending distally adjacent to the at leastone elongate guide, a platform disposed within the lumen, the platformincluding at least one projection, and a plunger.

Implementations of this Example may include one or more of the followingfeatures. The system where at least one actuator arm is in operationalcommunication with the at least one projection to translate linear forcefrom the arm into rotational force on the platform. The system where atleast one elongate guide includes a guide notch. The system where atleast one actuator arm includes an actuator catch. The system furtherincluding an actuation mechanism configured to increase platformresidence time. The system further including a membrane collar.

While multiple embodiments are disclosed, still other embodiments of thedisclosure will become apparent to those skilled in the art from thefollowing detailed description, which shows and describes illustrativeembodiments of the disclosed apparatus, systems and methods. As will berealized, the disclosed apparatus, systems and methods are capable ofmodifications in various obvious aspects, all without departing from thespirit and scope of the disclosure. Accordingly, the drawings anddetailed description are to be regarded as illustrative in nature andnot restrictive.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1A is a perspective external view of the collector, according toone embodiment.

FIG. 1B is a perspective view of the collector of FIG. 1A placed on theskin of a subject.

FIG. 2A is an exploded side view of an exemplary embodiment of thecollector.

FIG. 2B is a cross-sectional view of the embodiment of FIG. 2A.

FIG. 2C is an exploded side view of the collector according to analternative embodiment.

FIG. 2D is a cross-sectional view of the embodiment of FIG. 2C.

FIG. 3A is a perspective cross-sectional view of the internal componentsof the collector, according to one embodiment.

FIG. 3B is a cross-sectional view of the internal components, beforeactuation, according to the embodiment of FIG. 3A

FIG. 3C is a cross-sectional view of the internal components, duringactuation, according to the embodiment of FIG. 3A

FIG. 3D is a cross-sectional view of the internal components, afterretraction, according to the embodiment of FIG. 3A.

FIG. 4A is a side view of one embodiment of an actuation mechanism.

FIG. 4B is a side view of the actuation mechanism embodiment of FIG. 4A,during rotation.

FIG. 4C is a side view of the actuation mechanism embodiment of FIG. 4A,during rotation.

FIG. 4D is a side view of the actuation mechanism embodiment of FIG. 4A,during rotation.

FIG. 4E is a side view of the actuation mechanism embodiment of FIG. 4A,during retraction.

FIG. 5A is a side view of another embodiment of an actuation mechanism.

FIG. 5B is a side view of the actuation mechanism embodiment of FIG. 5A,during rotation.

FIG. 5C is a side view of the actuation mechanism embodiment of FIG. 5A,during rotation.

FIG. 5D is a side view of the actuation mechanism embodiment of FIG. 5A,during rotation.

FIG. 5E is a side view of the actuation mechanism embodiment of FIG. 5A,during retraction.

FIG. 6A a side view of the actuation mechanism comprising a guide notchembodiment.

FIG. 6B a further side view of the actuation mechanism comprisinganother guide notch embodiment.

FIG. 6C a further side view of the actuation mechanism comprisinganother guide notch embodiment.

FIG. 6D a further side view of the actuation mechanism comprising yetanother guide notch embodiment.

FIG. 7 is a histogram showing average time spent in the distal, firedposition according to several embodiments.

FIG. 8A is a top view schematic of the embodiment of FIG. 1A showing theprojection in the projection lock.

FIG. 8B is a top view schematic of the embodiment of FIG. 1A showing theprojection in the retraction position.

FIG. 8C is a top view schematic of the embodiment of FIG. 2A showing theprojection in the projection lock.

FIG. 8D is a top view schematic of the embodiment of FIG. 2A showing theprojection in the retraction position.

FIG. 9A is a perspective cross-sectional view of the button, housing andmembrane, according to an exemplary embodiment.

FIG. 9B is a perspective cross-sectional view of the membrane andplunger, according to an exemplary embodiment.

FIG. 10A is a perspective cutaway cross-sectional view of the plungerand membrane within the collector in the ready position, according to anexemplary embodiment.

FIG. 10B is a perspective cutaway cross-sectional view of the plungerand membrane within the collector in the actuated position, according toan exemplary embodiment.

FIG. 10C is a perspective cutaway cross-sectional view of the plungerand membrane within the collector in the retracted position, accordingto an exemplary embodiment.

FIG. 11A is a top schematic view of a membrane one embodiment of theone-way valve.

FIG. 11B is a top schematic view of a membrane another embodiment of theone-way valve.

FIG. 11C is a top schematic view of a membrane another embodiment of theone-way valve.

FIG. 11D is a histogram showing the vacuum pressure generated by theembodiments of FIGS. 11A-C.

FIG. 11E is a chart of the pressure profile for actuation and vacuumcreation over the course of actuation and retraction, according to anexemplary embodiment.

FIG. 12A is a close-up cross-sectional view of the bellows, according toan exemplary embodiment.

FIG. 12B is a close-up cross-sectional view of the membrane and plunger,according to an exemplary embodiment comprising ridges.

FIG. 13A is a cross-sectional view of a membrane, base, and plungeraccording to an exemplary embodiment.

FIG. 13B is a cross-sectional view of a membrane, base, and plungeraccording to an exemplary embodiment.

FIG. 14A is a close-up perspective cut-away view of a threshold stop,according to an exemplary embodiment.

FIG. 14B is a further close-up, three-quarters perspective cut-away viewof a threshold stop, according to an exemplary embodiment.

FIG. 14C is a further close-up, side cut-away view of a threshold stop,according to an exemplary embodiment.

FIG. 15A is a close-up perspective cut-away view of a threshold stop,according to another exemplary embodiment.

FIG. 15B is a further close-up, three-quarters perspective cut-away viewof the implementation of FIG. 15A.

DETAILED DESCRIPTION

The various embodiments disclosed or contemplated herein relate to asingle device that can be used by untrained or minimally-trained personsto both collect bodily fluid and seamlessly contain the bodily fluid,and related systems and methods. These devices, systems and methodsgenerally relate to a collector for bodily fluids having an actuator—or“button”—at one end and at least one lancet disposed within the oppositeend. In these implementations, when the button is depressed, anactuation mechanism is deployed—the lancets extend to pierce the skin ofa subject for the collection of fluid, and the actuator is disabled fromfurther use. Further description of the structure and function of theseembodiments is found herein.

It is understood that the various embodiments of devices, methods andsystems disclosed herein can be incorporated into or used with any otherknown medical devices, systems, and methods. For example, the variousembodiments disclosed herein may be incorporated into or used with anyof the medical devices and systems disclosed in co-pending U.S. Pat. No.9,289,763, filed Jul. 23, 2013, entitled “Methods, Systems, and DevicesRelating to Open Microfluidic Channels,” U.S. application Ser. No.14/932,485, filed Nov. 4, 2015, entitled “Methods, Systems, and DevicesRelating to Open Microfluidic Channels,” U.S. application Ser. No.13/750,526, filed Jan. 25, 2013, entitled “Handheld Device for Drawing,Collecting, and Analyzing Bodily Fluid,” and U.S. application Ser. No.14/816,994, filed Aug. 3, 2015, entitled Devices, Systems and Methodsfor Gravity-Enhanced Microfluidic Collection, Handling and Transferringof Fluids,” all of which are hereby incorporated herein by reference intheir entireties.

Turning to the figures with greater detail, FIGS. 1A-1B depict exemplaryembodiments of the gravity-enhanced fluid collection device, or simply“collector” 10. As is shown in FIGS. 1A-B, in exemplary embodiments, thecollector 10 generally comprises a housing 12 having proximal 12A anddistal 12B ends with an actuator 40 disposed there through, having apush button 42.

In use, the collector 10 provides for both the actuation and retractionof the collector's 10 internal components with a single application offorce to the actuator 40, or “button,” which passes into the collectorhousing 12 and comes to a rest. In exemplary embodiments, the collector10 is used to facilitate the puncture of the skin of a subject 1 forcollection of fluid in the reservoir 34 by way of a fitting or couplingportion 35, which is also called a “collar” in certain embodiments.

In exemplary embodiments, the reservoir 34 can be removably attached tothe housing 12, by way of the coupling portion 35, such that it may bedetached, as has been previously described in the incorporatedreferences. In certain embodiments, the reservoir 34 can be a standardEppendorf tube press-fitted on the fitting 35. In further embodiments,the reservoir 34 can also be custom made and utilize capillary forces orsolely gravitational forces to fill, as has also been previouslydescribed, such as in U.S. application Ser. No. 14/816,994, which hasbeen incorporated herein by reference. The tube 34 can thus act as aremovable and standardized reservoir 34 for containing or gathering thefluid that can be simply and easily detached and inserted into existingand established testing or lab equipment. By way of example, where thefluid is blood, the tube 34 can be easily inserted into clinical andlaboratory equipment or workflows for diagnostics and/or biomarkerdetections.

An exemplary embodiment of a collector 10 that can be used to bothcollect bodily fluid and contain the fluid is shown in FIGS. 2A-3C.FIGS. 2A-2D depict the internal components of the collector 10,according to various embodiments. FIGS. 3A-3C depict the variousinternal components of the collector 10 in use.

As shown generally in FIGS. 2A-2D, in these embodiments, the collector10 comprises a housing 12 that has an actuator 40, a platform 60, amembrane 80, a plunger 90 and a base 110. In exemplary embodiments,these components are disposed in operational communication through acentral lumen 18 of the housing 12 (as best shown in FIGS. 2B, 2D and3A), so as to facilitate the puncture of the skin of a subject at thedistal surface 120 of the base 110 for collection by way of lancets 130(as best shown in FIG. 3A), as is described herein. In use, thecollector 10 provides for both the actuation and retraction of thecollector's internal components with a single application of force tothe actuator 40, or “button,” which passes into the collector body 12and comes to a rest.

As shown in FIGS. 3A-C, the retraction phase extends the components—suchas the platform 60—proximally into the actuator 40 (shown in FIG. 3C),so as not to force the button 42 upwards. The retraction also results inthe creation of a vacuum within the membrane 80 so as to facilitatefluid draw, as is described further in relation to FIGS. 10A-10C. Asshown in FIGS. 4A-6D, in exemplary embodiments, the combined actuationand retraction is achieved by way of a translational movement of theinternal components over a prescribed distance, as will be described infurther detail below. Further, in exemplary embodiments, upon retractiona vacuum can be created within a sealed portion of the actuator.

Turning to the drawings in greater detail, in the implementations ofFIGS. 2A-3C, the collector 10 has a generally cylindrical housing 12with a proximal end 14 and a distal end 16. A generally cylindricalcentral lumen 18 is defined within the housing 12 between the proximalend 14 and a distal end 16, as best shown in FIGS. 2B and 2D. Anactuator 40 is disposed within the lumen 18, so as to be in operationalcommunication with a platform 60, as is described in further detail inrelation to FIGS. 4A-6D.

In these embodiments, as best shown in FIGS. 2A-2D, the actuator 40 hasa generally planar top button surface 42 and button wall 43, so as toform the “button” 42 which protrudes (shown at 40A) above the proximalend 14 of the housing while in the “ready” position as best shown inFIG. 3 (and as discussed below in relation to FIGS. 4A-4E, FIG. 10A andFIGS. 14A-14C). The button wall 43 is substantially enclosed by a lumenlip 15 (as best shown in FIGS. 2A, 2B and 3A), which is disposed aroundthe central lumen 18 at the proximal end 14 of the housing 12. Certainembodiments also feature a projection or threshold stop 45 as shown inFIGS. 2B and 2D. These components of the actuator 40 and housing 12 arediscussed further in relation to FIGS. 8A-8C.

Continuing with the implementations of FIGS. 2A-D, the central lumen 18has a plurality of elongate guides 20 disposed substantially from theproximal end 14 along the inner lumen surface 22. The elongate guides 20(as best shown in FIGS. 2B and 2D) depicted have a first guide end 24and a second guide end 26. In exemplary embodiments, the second guideend 26 further comprises a guide notch 28 and guide groove 30, thefunction of which are discussed below in relation to FIGS. 4A-4E. Thehousing 12 further comprises an outlet channel 32, which is configuredto couple with a collection tube 34 when assembled, as has beenpreviously described, for example in relation to U.S. application Ser.No. 14/816,994, which has been incorporated by reference.

In certain implementations, the actuator 40 can also have a plurality ofactuator arms 44 (shown in FIGS. 2B and 2D) further comprising a firstarm end 46 and second arm end 48—an arm opening 47 can be providedbetween the arms 46, 48 in certain implementations, as is shown in FIG.2A, FIG. 2B and FIG. 2D.

In various implementations, the actuator arms 44 extend distally fromthe underside 42A of the top button surface 42, and the second arm end48 further comprises an actuator notch 50 in these embodiments. Theactuator notch 50 is discussed further below in relation to FIGS. 4A-4Eand 5A-5E. In the embodiments of FIGS. 2B and 2D, the elongate guides 20of the housing 12 can be disposed adjacent to the actuator arms 44 ofthe button 40 (as discussed in relation to FIGS. 4A-E), or to theinterior of the lumen 18 relative to the actuator arms 44 (as is shownin FIG. 2D and discussed in relation to FIGS. 5A-5E), so as to be set“inside” the arms 44.

In the embodiments of FIGS. 2C-2D, an actuator catch 51 may also bedisposed at one end of the actuator notch 50. In these implementations,the actuator catch 51 can introduce a momentary delay in the actuationand retraction process that is desirable in certain implementations. Thevarious relationships of the elongate guides 20 to the actuator arms 44within the lumen 18 are described further in relation to FIGS. 4A-6D and8A-8D.

In various embodiments as best shown in FIGS. 2A-2D, the platform 60further comprises a top platform surface 62 and a generally cylindricalplatform wall 64 disposed around a platform lumen 66. In theseembodiments, the platform wall 64 further comprises a plurality ofplatform projections 70 disposed radially about the outer wall surface64A. In exemplary embodiments, these platform projections 70 are shapedin a manner which is complementary to the guide notch 28 and guidegroove 30 of the housing 12, and actuator notch 50 of the button 40, asdescribed in further detail below in relation to FIGS. 4A-6D. Inexemplary embodiments as shown in FIGS. 2A-D, the platform projections70 are disposed substantially at the distal wall end 72 of the platform60, though in alternative embodiments they can be disposed near the topplatform surface 62.

Turning to FIG. 3A, the platform 60 is configured to be disposed withinthe central lumen 18 when the collector 10 is assembled. The membrane 80is configured to be disposed within the platform lumen 66 when thecollector 10 is assembled, as best shown in FIG. 3A. The membrane 80according to certain implementations has a top membrane surface 82 and agenerally cylindrical membrane wall 84 disposed around a membrane lumen86. As shown in FIGS. 2A-2D, in exemplary embodiments, the membrane 80further comprises a substantially circular membrane lip 88 which isdisposed on the distal end of the membrane wall 84. In exemplaryembodiments, the membrane 80 and membrane lip 88 serve to create ahermetic and/or fluidic seal between a subject's skin (not shown) andthe membrane lumen 86, as is discussed below in relation to FIGS. 9A-9Cand FIGS. 10A-10C.

In the implementation of FIGS. 2A-3D, the plunger 90 is configured to bedisposed within the membrane lumen 86 when assembled, so as to be inoperational communication with the actuator 40, platform 60 and membrane80, as will be described in further detail below in relation to FIGS.4A-4E. In these embodiments, the plunger 90 and a spring 100 areconfigured to be housed within the base 110 in a generally cylindricalbase lumen 112. It is understood that in use, the base 110 is configuredto be disposed on underlying subject skin so as to create tension in theskin, thereby enhancing the ability to draw fluid through the collector10 and into the collection tube 34.

Continuing with the implementations of FIGS. 2A-3D, the plunger 90 has atop plunger surface 92 and a plurality of plunger bodies 94 which extenddistally from the underside 92A of the top plunger surface 92. Inexemplary embodiments, the plunger 90 has a plunger coupling lumen 96which is configured to mate with the base 110 on a base post 114. Inalternative embodiments, the plunger 90 can be aligned and guided by themembrane 80. In exemplary embodiments, the spring 100 is disposed aboutthe plunger 90 and within the base lumen 112 of the base 110 so as to becapable of urging the plunger 90 proximally.

When assembled, and as shown in FIGS. 3A-3D, the actuator 40 andplatform 60 are in operational communication so as to facilitate thedownward movement of the plunger 90, and accordingly the extension ofthe lancets 130 (shown in FIG. 3A) past the distal surface 120 (bestshown in FIGS. 1A-B) and into the subject's skin (not shown). In variousembodiments, and as shown in FIGS. 2A-B, the base 110 further comprisesone or more fluid collection passages, sometimes called a fluidic“network” 116.

In these implementations, the network or passages 116 are in fluidiccommunication with the base lumen 112, apertures 132 and collection tube34 so as to facilitate the movement of fluids from the collectionapertures 132 (as shown in FIG. 3A) to the collection tube 34, such asby way of open microfluidic channels, including those capable ofpromoting spontaneous capillary flow in U.S. application Ser. No.13/949,108 and the other teachings of the incorporated references above.It is understood that in various implementations the collectionapertures 132 are disposed within the base lumen 112 on the distalsurface 120 of the base 110.

FIGS. 3A-3DB show the assembled collector with the actuator 40 andinternal components in the “ready” position, meaning that the collector10 has not yet been actuated to collect any fluids, and the actuator 40is disposed in an “up” position in the lumen 15, adjacent to theproximal end 14 of the housing 12. As is further discussed below inrelation to FIGS. 8A-8C, the threshold stop 45 can function to preventthe movement of the actuator from the ready position absent theapplication of sufficient downward force from the user.

FIG. 3C-D depicts the collector 10 after actuation and retraction havebeen performed, such that the actuator 40 has been depressed(demonstrated with 40B), thereby urging the platform distally so as todepress the plunger 90 (shown in FIG. 3C) to the most distal position,followed by retraction of the platform 60 into the actuator lumen 41,shown in FIG. 3D, by way of the single actuation mechanism 150 describedin relation to FIGS. 4A-6D.

As can be seen in the implementations of FIGS. 4A-4E, the variouscollector 10 implementations have a self-locking, or single actuationmechanism 150, meaning a mechanism 150 that prevents repeated use of thecollector 10. In these implementations, the actuation mechanism 150facilitates the actuation and retraction of the internal components,keyed on the translation of linear movement into rotational movement,such that the platform 60 is able to rotate free of the elongate guides20/ actuator arms 44 and retract into the actuator lumen 41 by way ofthe spring 110 (as best shown in FIG. 3D).

As shown in the implementations of FIGS. 4A-6D, the mechanism 150 isformed by the substantial alignment of the previously discussed actuatorarms 44 of the button 40 and elongate guides 20 the housing 12. In theseembodiments, the single actuation mechanism 150 begins in a readyposition (prior to being deployed by depressing or otherwise actuatingthe actuator 40 and actuator arms 44) in relation to the platformprojections 60 as is shown in FIGS. 4A and 4D. As will be described indetail below, upon actuation, the single actuation mechanism 150 acts soas translate linear motion into rotational motion and transition to thefired state (where it can no longer be deployed) as is shown in FIGS. 4Cand 4E. In this way, the collector 10 is able to provide a single-use,self-locking actuation mechanism 150 and facilitates safe use.

In operation, the self-locking single actuation mechanism 150 isconfigured to prevent rotational movement of the platform 60. That is,while in the ready position (shown in FIG. 4A, FIG. 5A, FIG. 6A and 6D),a platform projection 70 is disposed within the projection lock 152,such that the proximal projection end 71 is nested within the projectionlock 152 to prevent any lateral movement. In certain embodiments, theprojection lock 152 is formed by the alignment of the actuator notch 50and guide groove 30 when the actuator (shown in FIG. 3A at 40) is in theready position (as is shown in FIGS. 3 and 4A). As is shown in FIGS.4A-4E, in these embodiments the actuator notch 50 comprises asubstantially planar notch face 50A which is set at an anglecomplementary to the planar projection face 70A, such that distalmovement of the actuator arms 44 will urge the projection 70 laterally.As is described in relation to FIGS. 4F-O, other configurations arepossible.

Returning to the embodiments of FIGS. 4A-E, the projection 70 andprojection lock 152 are of complementary shapes and configured such thatthe projection 70 is urged upwards by the force of the spring (thespring is shown in FIG. 2A at 100 and the force is depicted in FIGS.4A-4E as reference arrow A), so as to be nested or otherwise containedwithin the projection lock 152. In these implementations, the projection70 is held in a static position in the projection lock 152 when theactuator is in the ready position: the projection 70 (andcorrespondingly, the platform 60) is incapable of moving vertically orhorizontally (rotationally).

As is shown in FIG. 4B, when the button surface 42 is depressed, theactuation mechanism 150 urges the platform 60, represented by theprojection 70, through a distal and rotational actuation path. Theactuator arms 44 are urged distally (as is shown by reference arrow B).As shown in the figures, this distal movement disrupts the projectionlock 152, as in this embodiment the actuator notch 50 is displaceddistally relative to the guide groove 30, thereby imparting both adistal and rotational force on the projection 70 (rotational force shownby reference arrow C) due to the distal movement of the notch 50 pastthe distal tip of the groove 30. Collectively, the distal movement ofreference arrow B and rotational movement of reference arrow Caccordingly represent an embodiment of the “actuation path,” (which isalso shown variously in the figures at 154). As would be apparent to oneof skill in the art, the rotational resistance of the platform 60 aswell as the spring force can be adjusted to facilitate or prevent themovement of the projection 70 through the actuation path.

The rotational movement of the projection 70 in the actuation path (alsoshown in FIGS. 8A-8B) correspondingly moves the platform 60 bothdistally and rotationally, the distal movement being further impartedonto the plunger 90, as is shown in FIG. 4D, so as deploy the lancets(shown in FIG. 3 at 130) into the surface of a subject's skin. As wouldbe apparent to one of skill in the art, other configurations of theactuator notch 50, guide groove 30 and projection 70 can be utilized inthe single actuation mechanism 150.

As is shown in FIGS. 4C and 4E, upon sufficient rotational movement ofthe projection 70, the projection 70 moves out of alignment with theelongate guide 20, so as to next be urged proximally in the retractionpath 154. In certain embodiments, the guide notch 28 assists with therotational and vertical movement, by providing an angled plane 28A (asbest shown in FIG. 4C) which assists the projection 70 in so moving. Asis shown in FIG. 4E, because the projection 70, and therefore theplatform 60, is no longer within the projection lock 152, it is now freeto be urged upward by the spring force A past the projection lock 152.In this retraction path 154, the plunger 90 and correspondingly themembrane 80 (on the top plunger surface 92) can extend to a proximalposition that is further proximally than their proximal position when inthe ready position (as is shown in FIG. 4D, where the projection iswithin the projection lock 152).

FIGS. 5A-5E depict an alternative embodiment of the actuation mechanism150. In this embodiment, the actuator arm 44 has an actuator catch 51and the elongate guide 20 has a guide notch 28 to control the lateralmovement of the projection 70 (and correspondingly, the platform, as isshown in FIG. 3A). In these implementations, the actuator catch 51 isdisposed at one end of the actuator notch face 50A at a non-zero anglerelative to the notch face 50A. Accordingly, the actuator catch 51comprises a catch face 51A which is configured to impede the proximalprogress of the projection 70. Again, in these embodiments the actuatorarms 44 and elongate guides 20 can form the projection lock 152.However, in these embodiments the elongate guides 20 can also bedisposed to the interior of the device lumen relative to the actuatorarms 44 (as is also shown in FIG. 2B).

As is depicted in FIGS. 5A-5E, and as would be appreciated by a skilledartisan, when the actuator arm 44 (shown in FIG. 1A) is depressed, theprojection 70 is urged laterally in the direction of the catch 51 andacross the catch face 51A, the proximal progress of the proximalprojection end 71 is briefly retarded or delayed, thereby causing theprojection 70 and platform 60 to “springboard” slightly or otherwiseremain in the distal position slightly longer, thus increasing the totaltime that the plunger (shown in FIG. 10B) is in the distal position. Asis discussed below, there are advantages to this enhanced actuationduration.

As shown in FIG. 5A, in the ready position, the single actuationmechanism 150 is again configured to prevent the rotational movement ofthe platform 60. That is, while in the ready position the platformprojection 70 is disposed within the projection lock 152, which isformed by the guide groove 30 and optionally the actuator notch 50. Inexemplary embodiments, the projection 70 and projection lock 152 are ofcomplementary shapes and configured such that the projection 70 is urgedupwards by the force of the spring (shown as reference arrow A), so asto be nested within the projection lock 152, thereby again holding theprojection 70 and platform 60 in a static position.

As is shown in FIG. 5B-5C, when the button surface (shown in FIG. 1B at42) is depressed, the actuator arms 44 are urged distally in to thefiring state, thereby urging the platform 60 and projection 70 through adistal and rotational actuation path (shown at reference arrow C). Asshown in FIG. 5C, after the projection 70 has moved laterally, theproximal projection end 71 is brought into contact with the actuatorcatch 51. Accordingly, the proximal projection end 71 traverses thecatch face 51A, thereby delaying the proximal release and retraction ofthe platform while urging the actuator arm 44 proximally, as designatedby reference arrow D. In this embodiment, the proximal projection end 71continues laterally (reference arrow C) to the distal guide notch end28B (shown in FIGS. 5C-5D), such that the projection 70 is free to beurged upward by the spring force A past the projection lock 152 in FIG.5E.

FIGS. 6A-6D depict various embodiments of the single actuation mechanism150 comprising a variety of guide notch 28 configurations. FIG. 6Adepicts a guide notch 28 which is complementary to the angle of theplanar projection face 70A. In FIG. 6B, the guide notch 28C is disposedat an angle which is less than the angle of the projection face 70Aangle relative to the surface of the subject's skin (not shown). In thisembodiment, the guide notch 28C will induce greater relative downwardforce than lateral force, thereby slowing the lateral movement of theprojection 70 and increasing the time to retraction.

In FIGS. 6C-6D, the guide notches 28D, 28E feature a first guide face28F and second guide face 28G. In these configurations, the first guideface 28F can be of variable width (as shown by comparing FIG. 6C withFIG. 6D), and the second guide face 28G is angled so as to allow upwardprojection 70 movement, as has been previously described. In theseembodiments, the duration of actuation can thereby be controlled byrequiring the proximal projection end 71 to traverse the first guideface 28F laterally prior to freely releasing proximally.

FIG. 7 depicts the difference in residence time (in milliseconds) in theactuated state of the embodiments featuring an actuator catch 51 (asshown in FIGS. 5A-5E) as compared with the embodiments without a catch(FIGS. 4A-E) and the embodiments featuring a variable width guide face(FIGS. 6C-6D), that is, while the embodiment in FIGS. 4A-4E has anaverage residence time of 1 ms, the embodiment of FIGS. 5A-5E has anaverage residence time of 137 ms and the embodiment of FIGS. 6A-6D hasan average residence time of 317 ms.

As shown in FIGS. 8A-8B, the actuator arms 44 and elongate guides 20 aredisposed adjacently within the lumen 18 in the embodiments of FIGS. 1A,2A and 4A-E, both being positioned along the inner wall of the lumen 18.However, as shown in FIGS. 8C-8D, in the embodiments of FIGS. 1B, 2B and4F-J, the elongate guides 20 can be disposed centrally in the lumenrelative to the actuator arms 44 (that is, the elongate guides 20 can bedisposed further away from the inner wall of the lumen 18 and closer tothe center thereof).

Turning to the post-actuation retraction of these components, theproximal movement of the plunger and membrane can be utilized to createa vacuum within the collector 10 so as to facilitate fluid collection.FIGS. 9A-10C depict further views of the actuator 40 and housing 12, aswell as the membrane 80 and plunger 90. In exemplary embodiments, themembrane 80 is a unified membrane body 80 comprised of a single piece ofa flexible material, such as silicone, rubber, thermoplastic elastomer(“TPE”), thermoplastic vulcanizate (“TPV”), or thermoplasticpolyurethane (“TPU”), so as to be capable of flexible movement inresponse to the movement of the platform 60 and plunger 90, as isdescribed below in relation to FIGS. 10A-10C.

As is also shown in FIGS. 9A-15B, in exemplary embodiments of thecollector 10, the membrane 80 forms a fluidic and hermetic seal 87within the membrane lumen 86 (as best shown in FIGS. 10A-10D and 13B)around the plunger 90, collection apertures 132, base 110, distalsurface 120 and any network 116 of fluidic channels or passages fortransporting collected fluid to the collection tube 34 which may becontained therein. These implementations can incorporate any of thepreviously described methods, devices and systems, such as those forfluid collection, transport and storage in the incorporated references,including all disclosures in U.S. Pat. No. 9,289,763, U.S. applicationSer. Nos. 14/932,48, 13/750,526, and 14/816,994.

In these embodiments of FIGS. 9A-15B, the plunger 90 further comprises acentral valve opening 95. The central valve opening 95 is configured toallow the passage of gases through the plunger coupling 96 into themembrane lumen 86 as part of the one-way valve 160 described below.

As shown in FIG. 10A, the collector 10 is in the “ready” position. InFIG. 10B, the collector 10 has been actuated by a user depressing theactuator 40 such that the plunger 90 is in the most distal position as aresult. Movement of the plunger 90 to the distal position causes thelancets 130 to extend past the distal surface 120 of the base 110 (asbest shown in FIG. 10B) by way of the collection apertures 132. Throughthe actuation of the collector 10, the lancets 130 are able to piercethe skin of a subject and initiate the flow of fluid 200 into thecollection apertures 132, the passages or network 116 and eventuallyinto the collection tube 34 as has been previously described, forexample in relation to U.S. application Ser. No. 14/816,994, which hasbeen incorporated by reference in its entirety. The collection positionis also shown in FIG. 10C, wherein the plunger 90 has been extendedproximally past the ready position through the retraction path, andfluid 200 has been collected in the collection tube 34.

As discussed above and as shown in FIGS. 10A-20C, the creation of avacuum within the membrane lumen 86 can help to facilitate fluid flow.In certain embodiments, the membrane 80 further comprises a outletchannel 32 (best shown in FIG. 9B) which is configured to be in fluidicand hermetic communication with a collection tube (shown for example inFIGS. 1A-B at 34) or another collection system, as has been previouslydescribed, for example in relation to U.S. application Ser. No.14/816,994. In various implementations, a circular membrane lip 88 isprovided to be fixedly attached to the base 110 and create the hermeticand fluidic seal 87. In exemplary embodiments, the membrane lumen 86 canbe kept sterile as a result of the seal 87, while the remaining aspectsof the central lumen need not be.

Importantly, because the membrane 80 is flexible and can be deformed andthereby cause the interior volume of the membrane lumen 86 to change,this volume change can alter the pressure inside the fluidic andhermetic seal 87 of the lumen 86. In exemplary embodiments as best shownin FIG. 9B, the membrane 80 further comprises a one-way valve 160configured to allow the air contained within the membrane lumen 86 toescape in response to the downward motion of the platform 60. In someimplementations, this one-way valve 160 can be made up of at least oneslit 161. As shown in FIGS. 10A-11C, in various embodiments, the one-wayvalve 160 can have one or more one-way valve openings 166 or slits 161disposed about the top membrane surface 82 in a variety ofconfigurations, such as those shown in FIGS. 11A-C. Other embodimentsare possible, as would be apparent to one of skill in the art.

Returning to FIG. 10B, in response to actuation, the plunger 90 is urgeddistally, and the membrane 80 is compressed. However, the pressureinside the membrane lumen 86 stays at substantially atmospheric pressureas air within the membrane lumen 86 is urged out of the central valveopening 95 and through the slits 161 or openings 166 of the one-wayvalve 160. The central lumen (shown in FIGS. 2A-2B at 18) also continuesto be at or near atmospheric pressure when it is deformed distally bythis movement, as there is no such seal around the platform 60, orbetween the actuator 40 and housing 12. At substantially the same time,the lancets 130 puncture the skin of the subject, thereby inducing fluidcollection from the subject's skin.

Following the completion of the actuation process, and as shown in FIG.10C, the plunger 90 is urged proximally through the retraction path byway of spring 100, as described above in relation to FIGS. 4C and 4E.This upward, proximal movement of the plunger 90 causes a correspondingmovement of the top membrane surface 82 away from the circular membranelip 88 and distal surface 120 of the base 110 (shown in FIGS. 1A-B).This movement results in an expansion of the membrane lumen 86 volume.The one-way valve 160 (which could be slits 161 or one-way valveopenings 166 disposed in a variety of configurations, as shown in FIGS.11A-C) prevents air from entering the membrane lumen 86. The resultingpressure drop within the membrane lumen 86 creates a vacuum relative toatmospheric pressure, thereby encouraging fluid flow from the subjectinto the collection apertures 132. Again, this is because the one-wayvalve 160 is configured such that it does not allow air to enter themembrane lumen 86. As such, the post-actuation retraction can create avacuum which facilitates fluid collection.

Certain embodiments of the top membrane surface 82 have bellows 162,which facilitate the movement of the membrane 80 and the increase involume of the membrane lumen 86, as is shown in FIGS. 10A-10C. In theseembodiments, the bellows 162 can allow the membrane 80 to easily movebetween the various positions without unnecessary stretching of themembrane 80. This allows for air to be more efficiently moved out of themembrane lumen 86, and can guide the plunger 90 distally and proximallythrough the actuation and retraction paths, respectively. Accordingly,this movement of the bellows 162 can be achieved without impeding theoperational path of the plunger 90 as it moves along the cylindricalmembrane wall 84.

As shown in FIGS. 11A-11C, various one-way valve 160 configurationsfeaturing one or more slits 161 or openings 166 are possible,respectively. FIG. 11D demonstrates that each of these various membrane80 configurations can result in variations in the vacuum pressuregenerated in kPa.

The pressure profile for actuation and vacuum creation is shown in FIG.11E. In this example, the pressure inside the membrane 80 was assessedduring actuation and retraction of the device over time in kPa. Theresults demonstrate the initial increase in pressure inside the device,which is followed by an extended period of vacuum pressure which remainsrelatively constant, but in certain embodiments can decay slightly overthe course of the 20 seconds shown. As would be apparent to one of skillin the art, and as previously discussed, the creation of this vacuumwithin the device facilitates blood draw.

In the embodiment of FIG. 12A, the bellows 162 utilize a rollingmembrane design. This design is a U-shaped membrane (shown at 162) thatallows the bellows 162 to roll along the outer wall 167 and inner wall168 during actuation (as shown in FIGS. 10A-10C). In exemplaryembodiments, the bellows are configured to elongate during retraction toallow a vacuum to be created inside the membrane lumen 86. Stiffermaterials, such as those which exceed Shore 30A can be effective duringthe air expulsion process. As is also shown in FIG. 12A, in certainembodiments the plunger 90 comprises a membrane opening 98, which isconfigured to secure a membrane component member 169. In theseimplementations, the member 169 is a portion of the membrane that isfitted into the opening in the manner of a plug, so as to provideenhanced membrane 80 and bellows 162 stability and to facilitate thecreation of a proper seal within the membrane lumen 86.

In various alternate embodiments, and that of FIG. 12B, the connectionbetween the membrane 80 and plunger 90 can comprise at least one ridgeon the plunger's proximal face 90A. In this embodiment, the plunger 90has an inner ridge 91 which is adjacent to the central valve opening 95and an outer ridge 93 which is adjacent to the bellows 162. In theseembodiments, the inner ridge 91 can facilitate the creation of a sealbetween the membrane 80 and plunger 90 to facilitate the opening andclosing of the valve slit 161 or opening 166.

As shown in FIG. 12B, the outer ridge 93 can prevent tenting by reducingor eliminating the development of tension between the membrane 80 andthe inner ridge 91 (designated in FIG. 12B as the membrane portion 81).During actuation, the platform 60 is urged distally (shown at referencearrow B) and then, during retraction, proximally by the force of thespring (shown as reference arrow A). During actuation and retraction,tension can develop in the membrane portion 81, and this tension canlimit the ability of the membrane 80 to release air during the actuationprocess (described above in relation to FIGS. 9A-11E).

Accordingly, as shown in FIG. 12B, the outer ridge 93 is configured toalign the portion of the membrane 80 between the inner ridge 91 andouter ridge into a plane (shown by reference line M) which issubstantially perpendicular from the direction of actuation (shown byreference arrows A and B), thereby preventing tenting about the innerridge 91.

In the implementation of FIG. 13A, the base 110 further comprises amembrane collar 83 fitted around the membrane 80. In theseimplementations, the relatively rigid membrane collar 83 serves tocompress or otherwise secure the flexible membrane 80 around the plunger90.

It is understood that the membrane collar 83 can be effective inmaintaining the membrane seal 87 and preventing the expulsion of airfrom the membrane other than through the one-way valve. In theseimplementations, the membrane collar 83 also prevents the “rubbing” ofthe platform 60 on the membrane 80.

In FIG. 13B, a membrane 80 having an operationally integrated overmold89 is shown. In these implementations, the top, flexible portioncomprises an elastomer membrane 89A, which extends distally around theplunger, where it is integrated with an a rigid lower flange 89B. Invarious implementations, the lower flange 89B is polypropylene, or someother similar material.

As is shown in FIGS. 14A-14C, in certain embodiments, the actuator 40has a threshold stop 45. In exemplary embodiments, the threshold stop 45is a protrusion 45A disposed on the button wall 43. Prior to use, theactuator's button 40A is positioned above the proximal end 14 of thehousing 12 in the “ready” position, the button wall 43 further beingsubstantially aligned with the lumen lip 15 of the housing, which isdescribed above. As is shown in FIGS. 14A-14C, the protrusion 45A isdisposed so as to abut against the lumen lip 15 on the top side 15A.

In the embodiments of FIGS. 14A-14C, the threshold stop 45 and/or lumenlip 15 can be comprised of deformable materials, such as thermoplastics(such as polypropylene, polyethylene, or acrylonitrile butadiene styrene(“ABS”), or TPEs, so as to physically prevent the distal movement of theactuator 40 unless a force sufficient to deform the threshold stop 45and/or lumen lip 15 is applied. This threshold force requirement therebyholds the actuator 40 in the “ready” position absent the application ofsufficient downward, or distal, force to the button 40A. In alternativeembodiments, the threshold stop 45 can be made of materials known in theart to fracture in response to a threshold force.

In various alternate implementations, and as shown in FIGS. 15A-15B, thethreshold stop 45 is disposed at the end of at least one elongate,cantelevered arm 170. Unlike the implementations of FIGS. 14A-14C, thecantelevered arm 170 in these implementations are disposed inside thelumen 18, further away from the cover 12 as opposed to on the surface ofthe button 40, as shown in FIGS. 14A-14C. In this implementation, thethreshold stops 45 are in operational communication with the platform60, as opposed to the button 40, thereby keeping the whole subassemblytogether as a subunit, further simplifying the assembly process byallowing the unit to remain static during movement in the assemblyprocess. It is understood that this configuration allows for largerthreshold stops 45 and higher or lower tolerances in press force.

Because a sufficient force is required to cause actuation in theseembodiments, the collector 10 can both prevent accidental actuation andensure that the actuation force applied is sufficient to break the skinof the subject and result in a fluid draw. Further, because theactuation path is independent from the retraction path (as describedabove in relation to FIGS. 4A-4E), the internal components of thecollector 10 can be brought to a position that cannot be re-actuated,thereby preventing subsequent use.

Further, the collector 10 allows for the ability to control the amountof force, and correspondingly the velocity, required for actuation. Thisis because the threshold stop 45 and the actuation mechanism 150 can becontrolled by way of the platform 60 rotation and spring resistancedescribed above in relation to FIGS. 4A-4E. The control allows for theprecise determination of lancet 130, or needle penetration into asubject's skin. This is because the engineered lancet throw distance canimpact the volume and type of bodily fluid extracted from the tissue, inparticular ratio of blood to interstitial fluid which is drawn. Incertain embodiments, this engineered distance can be between 1 mm and 5mm.

Although the disclosure has been described with reference to preferredembodiments, persons skilled in the art will recognize that changes maybe made in form and detail without departing from the spirit and scopeof the disclosed apparatus, systems and methods.

What is claimed is:
 1. A collector, comprising: a. a housing comprisingproximal and distal ends and a lumen; b. an actuator disposed within thelumen; c. a platform disposed within the lumen and distal to theactuator; d. single use actuation mechanism in operational communicationwith the platform; and e. a plunger comprising at least one lancet,wherein the single actuation mechanism is configured to translate linearforce applied to the actuator into rotational force on the platform andurge the plunger distally.
 2. The collector of claim 1, furthercomprising a membrane disposed within the lumen, wherein the membrane isconfigured to create a fluidic seal within the lumen.
 3. The collectorof claim 2, wherein the membrane comprises a membrane lumen and a oneway valve configured to create a vacuum within the membrane lumen. 4.(The collector of claim 2, wherein the membrane comprises a bellows. 5.The collector of claim 2, wherein plunger is configured to retract afteractuation.
 6. The collector of claim 2, wherein the platform comprisesat least one projection which is in operational communication with thesingle actuation mechanism.
 7. The collector of claim 6, wherein thesingle actuation mechanism comprises at least one actuator arm and atleast one elongate guide.
 8. The collector of claim 7, wherein thesingle actuation mechanism is configured so as rotate the platformduring actuation by way of the projection.
 9. A single use fluidcollector, comprising: a. a housing comprising proximal and distal endsand a lumen; b. an actuator comprising at least one actuator armdisposed within the lumen; and c. a platform comprising at least oneprojection disposed within the lumen and distal to the actuator; whereinthe at least one actuator arm is in translational and rotationalcommunication with the platform via the at least one projection.
 10. Thecollector of claim 9, wherein the housing comprises at least oneelongate guide comprising a guide groove.
 11. The collector of claim 10,further comprising a spring configured urge the at least one projectioninto the guide groove.
 12. The collector of claim 11, wherein the atleast one actuator arm is configured to urge the projection distally anddislodge it from the guide groove in response to actuation.
 13. Thecollector of claim 12, further comprising a variable width guide face.14. The collector of claim 12, wherein the at least one projectioncomprises a projection face configured to rotate the platform when theprojection is urged distally.
 15. An actuation and retraction system foruse in a medical device, the system comprising: a. a housing comprisinga central lumen extending through the housing and comprising at leastone elongate guide disposed within the central lumen; b. an actuatorcomprising at least one actuator arm extending distally adjacent to theat least one elongate guide; c. a platform disposed within the lumen,the platform comprising at least one projection; and d. a plunger. 16.The system of claim 15, wherein at least one actuator arm is inoperational communication with the at least one projection to translatelinear force from the arm into rotational force on the platform.
 17. Thesystem of claim 15, wherein at least one elongate guide comprises aguide notch.
 18. The system of claim 15, wherein at least one actuatorarm comprises an actuator catch.
 19. The system of claim 15, furthercomprising an actuation mechanism configured to increase platformresidence time.
 20. The system of claim 15, further comprising amembrane collar.